Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0696113
Disease: Serum ferritin measurement
Serum ferritin measurement 		10 21 10 1.00 21 1.00
CUI: C0337439
Disease: Iron measurement
Iron measurement 		12 16 3 0.16 3 8.8E-02
CUI: C0428578
Disease: Iron level result
Iron level result 		12 16 3 0.16 3 8.8E-02
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 10 2 0.14 3 0.11
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 10 2 0.14 3 0.11
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		7 26 2 0.13 3 6.8E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		17 25 3 0.12 4 9.5E-02
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		10 19 2 0.11 2 5.3E-02
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 2 0.11 2 9.1E-02
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 1.0E-01 1 4.8E-02
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 1.0E-01 0 0
CUI: C1857810
Disease: Deafness, prelingual, profound (affects all frequencies)
Deafness, prelingual, profound (affects all frequencies) 		1 0 1 1.0E-01 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 1.0E-01 1 4.8E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 1.0E-01 1 4.8E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 1.0E-01 2 9.5E-02
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 1.0E-01 1 4.8E-02
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 1.0E-01 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 2 1 1.0E-01 2 9.5E-02
CUI: C3892050
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 102
DEAFNESS, AUTOSOMAL RECESSIVE 102 		1 0 1 1.0E-01 0 0
CUI: C4522164
Disease: HELIX SYNDROME
HELIX SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C4540185
Disease: SPERMATOGENIC FAILURE 23
SPERMATOGENIC FAILURE 23 		1 0 1 1.0E-01 0 0
CUI: C4703592
Disease: Elevated hepcidin level
Elevated hepcidin level 		1 0 1 1.0E-01 0 0
CUI: C4748725
Disease: RETINITIS PIGMENTOSA 84
RETINITIS PIGMENTOSA 84 		1 0 1 1.0E-01 0 0
CUI: C0151861
Disease: Porphyruria
Porphyruria 		2 0 1 9.1E-02 0 0
CUI: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 6 1 9.1E-02 2 8.0E-02